Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
- Keyword register: select an initial character and browse associated keywords
- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. You can export your saved items to PDF by clicking the download icon.
Indian J. Pharm. Sci. 69 (4), 578 (2007). TLC of tinosporaside in defatted methanolic extracts of Tinospora Cordifolia stem bark on silica gel with toluene - acetone -water 5:15:1. Quantitative evaluation by densitometry at 220 nm. The method was found to be linear in the range of 0.5-8 mg. Recovery was 99.3%. The stem bark of the plant contained 0.4 % of tinosporaside.
J. AOAC Int. 90, 1573-1578 (2007). TLC of olanzapine [2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b] [1,5]benzodiazepine] and fluoxetine [(+/-)-N-methyl-3-phenyl-3-[(alpha,alpha,alpha-trifluoro-p-tolyl)oxy]propylamine] on silica gel using methanol - toluene 2:1 in a twin-trough chamber with chamber saturation. Quantitation by densitometry in absorption mode at 233 nm.
59th Indian Pharmaceutical congress F-11, 392, (2007). HPTLC oleanloic acid from seeds of Achyranthes aspera on silica gel with n-hexane - ethyl acatete - acetic acid 30:201. Detection by spraying with anisaldehyde - sulphuric acid reagent. Densitometry at 530 nm for quantification of oleanolic acid. Linearity was between 200 and 1200 ng/zone. The plant tree was found to contain 0.34 % oleanloic acid. The method can be used for routine quality control.
CBS 100, 6-7 (2008). HPTLC of the alkaloid deoxypeganine (from Peganum harmala) and bromination reaction products on silica gel over 60 mm with chloroform - methanol - acetone - cyclohexane 5:1:5:5 for Merck phases and 4:1:4:4 for Whatman phases. Quantitative determination by absorbance measurement at 254 nm.
Indian Drugs 44 (12), 937-944 (2007). HPTLC of methanolic and ethyl acetate extracts of Sesamum indicum root on silica gel with ethyl acetate - n-hexane 1:9. Densitometric evaluation at 549 nm. The red zones were isolated by preparative TLC and identified by IR as 1,4 naphthoquinone derivatives.
J. Planar Chromatogr. 21, 103-106 (2008). HPTLC of (-)-epicatechin, (+)-catechin, (-)-epigallocatechin, (-)-gallocatechin, (-)-catechin gallate, and (-)-epicatechin gallate on RP-18 at room temperature and 75 % relative humidity in an automated development chamber with methanol - water - formic acid 30:70:6. Detection by spraying with diazotized sulfanilic acid. Quantitation by densitometry at 440 nm.
J. AOAC Int. 91, 1191-1195 (2008). HPTLC of ketorolac tromethamine ((+/-)-5-(benzoyl)-2,3-dihydro-1N-pyrrolizine-1-carboxylic acid tris hydroxymethylaminomethane) on silica gel prewashed with methanol with n-butanol - chloroform - acetic acid - ammonium hydroxide - water 9:3:5:1:2 in a horizontal developing chamber. Quantitative determination by absorbance measurement at 323 nm.
J. Chromatogr. A 1207 (1-2), 155-159 (2008). HPTLC of secoisolariciresinol diglucoside in flaxseed on RP18W with methanol - 0.1 % formic acid 2:3, using the alkaline hydrolysis in aqueous medium of undefatted samples. Quantitative determination by absorbance measurement at 282 nm. Validation of the method following the protocol proposed by the Société Francaise des Sciences et Techniques Pharmaceutiques lead to a dependable and high throughput procedure well suited for routine application. Linearity was between 321–1071 ng/zone and the RSD of repeatability and intermediate precision did not exceed 3.6 %.